Scientific theory and agricultural practice : Plant breeding in Germany from the late 19th to the early 20th centuryWIELAND, Thomas.Journal of the history of biology. 2006, Vol 39, Num 2, pp 309-343, issn 0022-5010, 35 p.Article

Enhanced Sarcoplasmic Reticulum Ca²⁺ Leak and Increased Na⁺-Ca²⁺ Exchanger Function Underlie Delayed Afterdepolarizations in Patients With Chronic Atrial FibrillationVOIGT, Niels; NA LI; WEHRENS, Xander H. T et al.Circulation (New York, N.Y.). 2012, Vol 125, Num 17, pp 2059-2070, issn 0009-7322, 12 p.Article

Angiotensin II type 2 receptor inhibits vascular endothelial growth factor-induced migration and in vitro tube formation of human endothelial cellsBENNDORF, Ralf; BOGER, Rainer H; ERGÜN, Süleyman et al.Circulation research. 2003, Vol 93, Num 5, pp 438-447, issn 0009-7330, 10 p.Article

Expression of ten RGS proteins in human myocardium: functional characterization of an upregulation of RGS4 in heart failureMITTMANN, Clemens; CHIN HEE CHUNG; HIRT, Stephan et al.Cardiovascular research. 2002, Vol 55, Num 4, pp 778-786, issn 0008-6363Article

Highly Invasive Melanoma Cells Activate the Vascular Endothelium via an MMP-2/Integrin αvβ5-Induced Secretion of VEGF-ADESCH, Anna; STROZYK, Elwira A; BAUER, Alexander T et al.The American journal of pathology. 2012, Vol 181, Num 2, pp 693-705, issn 0002-9440, 13 p.Article

Role of RyR2 Phosphorylation at S2814 During Heart Failure ProgressionRESPRESS, Jonathan L; OORT, Ralph J. Van; WISLØFF, Ulrik et al.Circulation research. 2012, Vol 110, Num 11, pp 1474-1483, issn 0009-7330, 10 p.Article

β-Adrenergic receptor stimulation causes cardiac hypertrophy via a Gβγ/Erk-dependent pathwayVIDAL, Marie; WIELAND, Thomas; LOHSE, Martin J et al.Cardiovascular research. 2012, Vol 96, Num 2, pp 255-264, issn 0008-6363, 10 p.Article

Displaced Fractures of the Greater Tuberosity : A Comparison of Operative and Nonoperative TreatmentPLATZER, Patrick; THALHAMMER, Gerhild; OBERLEITNER, Gerhard et al.The Journal of trauma, injury, infection, and critical care. 2008, Vol 65, Num 4, pp 843-848, issn 1079-6061, 6 p.Article

Calmodulin Mutations Associated With Recurrent Cardiac Arrest in InfantsCROTTI, Lia; JOHNSON, Christopher N; PEDRAZZINI, Matteo et al.Circulation (New York, N.Y.). 2013, Vol 127, Num 9, pp 1009-1017, issn 0009-7322, 9 p.Article

Reduced viability of neuronal cells after overexpression of protein histidine phosphataseKRIEGLSTEIN, Josef; LEHMANN, Martina; MÄURER, Anette et al.Neurochemistry international. 2008, Vol 53, Num 5, pp 132-136, issn 0197-0186, 5 p.Article

Protein kinase D selectively targets cardiac troponin I and regulates myofilament Ca²⁺ sensitivity in ventricular myocytesCUELLO, Friederike; BARDSWELL, Sonya C; HAWORTH, Robert S et al.Circulation research. 2007, Vol 100, Num 6, pp 864-873, issn 0009-7330, 10 p.Article

The BTB-kelch protein KLEIP controls endothelial migration and sprouting angiogenesisNACAK, Tanju G; ALAJATI, Abdullah; KROLL, Jens et al.Circulation research. 2007, Vol 100, Num 8, pp 1155-1163, issn 0009-7330, 9 p.Article

Background data acquisition and carrying : The BlueDACS projectWIELAND, Thomas; FENNE, Martin; STOCKER, Benjamin et al.Lecture notes in computer science. 2006, pp 56-68, issn 0302-9743, isbn 3-540-32765-7, 1Vol, 13 p.Conference Paper

Exome Sequencing Identifies a REEP1 Mutation Involved in Distal Hereditary Motor Neuropathy Type VBEETZ, Christian; PIEBER, Thomas R; VARGA, Rita-Eva et al.American journal of human genetics. 2012, Vol 91, Num 1, pp 139-145, issn 0002-9297, 7 p.Article

Lack of the Mitochondrial Protein Acylglycerol Kinase Causes Sengers SyndromeMAYR, Johannes A; HAACK, Tobias B; MORONI, Isabella et al.American journal of human genetics. 2012, Vol 90, Num 2, pp 314-320, issn 0002-9297, 7 p.Article

Regulation of cardiac cAMP synthesis and contractility by nucleoside diphosphate kinase B/G protein βγ dimer complexesHIPPE, Hans-Joerg; LUEDDE, Mark; LUTZ, Susanne et al.Circulation research. 2007, Vol 100, Num 8, pp 1191-1199, issn 0009-7330, 9 p.Article

Endotoxin induces desensitization of cardiac endothelin-1 receptor signaling by increased expression of RGS4 and RGS16PATTEN, Monica; BÜNEMANN, Jan; THOMA, Bryan et al.Cardiovascular research. 2002, Vol 53, Num 1, pp 156-164, issn 0008-6363Article

Constitutive Activation of PKA Catalytic Subunit in Adrenal Cushing's SyndromeBEUSCHLEIN, Felix; FASSNACHT, Martin; SCHAAK, Katrin et al.The New England journal of medicine. 2014, Vol 370, Num 11, pp 1019-1028, issn 0028-4793, 10 p.Article

Impaired riboflavin transport due to missense mutations in SLC52A2 causes Brown-Vialetto-Van Laere syndromeHAACK, Tobias B; MAKOWSKI, Christine; YOSHIMATSU, Hiroki et al.Journal of inherited metabolic disease. 2012, Vol 35, Num 6, pp 943-948, issn 0141-8955, 6 p.Article

Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsyWINKELMANN, Juliane; LING LIN; POLI, Francesca et al.Human molecular genetics (Print). 2012, Vol 21, Num 10, pp 2205-2210, issn 0964-6906, 6 p.Article

Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIAHAACK, Tobias B; HOGARTH, Penelope; CUNO, Stephan M et al.American journal of human genetics. 2012, Vol 91, Num 6, pp 1144-1149, issn 0002-9297, 6 p.Article

Superiority of voriconazole over amphotericin B in the treatment of invasive aspergillosis after heart transplantationWIELAND, Thomas; LIEBOLD, Andreas; JAGIELLO, Magda et al.The Journal of heart and lung transplantation. 2005, Vol 24, Num 1, pp 102-104, issn 1053-2498, 3 p.Article

Molecular diagnosis in mitochondrial complex I deficiency using exome sequencingHAACK, Tobias B; HABERBERGER, Birgit; HENNERMANN, Julia B et al.Journal of medical genetics. 2012, Vol 49, Num 4, pp 277-283, issn 0022-2593, 7 p.Article

DHTKD1 Mutations Cause 2-Aminoadipic and 2-Oxoadipic AciduriaDANHAUSER, Katharina; SAUER, Sven W; MEITINGER, Thomas et al.American journal of human genetics. 2012, Vol 91, Num 6, pp 1082-1087, issn 0002-9297, 6 p.Article

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing studyRAUCH, Anita; WIECZOREK, Dagmar; DUFKE, Andreas et al.Lancet (British edition). 2012, Vol 380, Num 9854, pp 1674-1682, issn 0140-6736, 9 p.Article